National Marine Fisheries Research Institute, Kołłątaja 1 Street, 81-332, Gdynia, Poland.
Department of Water and Soil Analysis, Faculty of Chemistry, Adam Mickiewicz University in Poznań, Umultowska 89b Street, 61-614, Poznań, Poland.
Environ Sci Pollut Res Int. 2017 Oct;24(29):23026-23038. doi: 10.1007/s11356-017-9932-2. Epub 2017 Aug 19.
Measurements of trace element (As, Cu, Cd, Cr, Ni, Pb, Zn) deposition fluxes were conducted simultaneously in two contrasted environments, i.e., urban and forest, between April 2013 and October 2014. This was the first such project in central Poland, aimed at long-term observations of trace elements in the atmosphere and their distribution, transport, and deposition pattern. The receptor sites were different in terms of local meteorological conditions, emission potential, and distance to major anthropogenic sources. The deposition fluxes of all trace elements showed clear seasonal variations, with relatively higher values in winter than in summer. The main factors affecting interannual differences in concentrations and deposition of trace elements in central Poland were local emission from industrial and commercial sources, and changes in atmospheric conditions (wind speed and direction, boundary layer, precipitation amount, air mass origin). In this study, the impact of regional and long-range transport on trace element deposition was determined using the air back-trajectory cluster analysis. During the summertime of 2013 and 2014, the predominant SW and E advections from regional and remote anthropogenic sources in Europe were responsible for high deposition of Cd, Cr, Pb, Cu, and Zn, whereas during the wintertime of 2013/2014, we observed a significant influence of polluted air masses from southeastern regions. Based on the Pb/Zn ratio, it was found that regional sources significantly influenced the aerosol composition and rainwater chemistry within the study domain. However, the role of a long-range transport of anthropogenic pollutants was also important. In addition, a relatively small difference in the Pb/Zn ratio between both sites (urban 0.26 ± 0.18, forest 0.23 ± 0.17) may suggest (1) very similar contribution of anthropogenic sources and (2) minor importance of atmospheric transformation processes of these metals in the aqueous phase.
我们于 2013 年 4 月至 2014 年 10 月在两个截然不同的环境(城市和森林)中同时进行了痕量元素(As、Cu、Cd、Cr、Ni、Pb、Zn)沉积通量的测量。这是波兰中部首次开展此类项目,旨在对大气中痕量元素及其分布、传输和沉积模式进行长期观测。受体站点在局部气象条件、排放潜力和与主要人为源的距离方面存在差异。所有痕量元素的沉积通量均表现出明显的季节性变化,冬季相对高于夏季。影响波兰中部痕量元素浓度和沉积的年际差异的主要因素是工业和商业源的本地排放以及大气条件(风速和风向、边界层、降水量、气团来源)的变化。在本研究中,使用空气后轨迹聚类分析确定了区域和长距离传输对痕量元素沉积的影响。在 2013 年和 2014 年的夏季,来自欧洲区域和远程人为源的 SW 和 E 平流导致 Cd、Cr、Pb、Cu 和 Zn 的沉积量较高,而在 2013/2014 年的冬季,我们观察到受污染空气团从东南地区的显著影响。基于 Pb/Zn 比值,发现区域源显著影响了研究区域内气溶胶组成和雨水化学。然而,人为污染物长距离传输的作用也很重要。此外,两个站点(城市 0.26±0.18,森林 0.23±0.17)之间 Pb/Zn 比值的相对较小差异可能表明(1)人为源的贡献非常相似,(2)这些金属在水相中的大气转化过程的重要性较小。